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Volumn 11, Issue 11, 2003, Pages 2395-2402
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Benzothiadiazine dioxides (BTD) derivatives as non-nucleoside human cytomegalovirus (HCMV) inhibitors. Study of structural requirements for biological activity
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Author keywords
[No Author keywords available]
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Indexed keywords
1 (PHENYLBUTYL) 3 BENZYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(3,4 DICHLOROPHENYL)METHYL] 3 BENZYL 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(3,4 DICHLOROPHENYL)METHYL] 3 ETHYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(3,4 DICHLOROPHENYL)METHYL] 3 ISOBUTYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(3,4 DICHLOROPHENYL)METHYL] 4 (CYCLOHEXYLMETHYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(3,4 DICHLOROPHENYL)METHYL] 4 (ISOBUTYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(3,4 DICHLOROPHENYL)METHYL] 4 (ISOPROPYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(4 BROMOPHENYL)CARBONYLMETHYL] 3 BENZYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 3 CYCLOHEXYLMETHYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 3 ETHYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 3 ISOBUTYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 3 ISOPROPYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 3 METHYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 3 PROPARGYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 3 PROPYL 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 4 (CYCLOHEXYLMETHYLOXY) 2,1,3 BENZOTHIADIAZIN 4 ONE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 4 (ETHYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 4 (ISOBUTYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 4 (ISOPROPYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 4 (METHYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
1 [(4 CHLOROPHENYL)METHYL] 4 (PROPYLOXY) 2,1,3 BENZOTHIADIAZINE 2,2 DIOXIDE;
ANTIVIRUS AGENT;
BENZOTHIADIAZINE DERIVATIVE;
UNCLASSIFIED DRUG;
ANTIVIRAL ACTIVITY;
ARTICLE;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HOST CELL;
HUMAN;
HUMAN CELL;
HUMAN CYTOMEGALOVIRUS;
IC 50;
STRUCTURE ACTIVITY RELATION;
HUMAN HERPESVIRUS 5;
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EID: 0037624825
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/S0968-0896(03)00148-2 Document Type: Article |
Times cited : (8)
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References (20)
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